المؤلفون: Blauwendraat, C., Faghri, F., Pihlstrom, L., Geiger, J. T., Elbaz, A., Lesage, S., Corvol, J. -C., May, P., Nicolas, A., Abramzon, Y., Murphy, N. A., Gibbs, J. R., Ryten, M., Ferrari, R., Bras, J., Guerreiro, R., Williams, J., Sims, R., Lubbe, S., Hernandez, D. G., Mok, K. Y., Robak, L., Campbell, R. H., Rogaeva, E., Traynor, B. J., Chia, R., Chung, S. J., Hardy, J. A., Brice, A., Wood, N. W., Houlden, H., Shulman, J. M., Morris, H. R., Gasser, T., Kruger, R., Heutink, P., Sharma, M., Simon-Sanchez, J., Nalls, M. A., Singleton, A. B., Scholz, S. W., Noyce, A. J., Giri, A., Oehmig, A., Tucci, A., Schulte, C., Cookson, M. R., Kia, D., Danjou, F., Charlesworth, G., Plun-Favreau, H., Holmans, P., Jansen, I., Hardy, J., Bras, J. M., Quinn, J., Botia, J. A., Billingsley, K., R'Bibo, L., Lungu, C., Martinez, M., Escott-Price, V., Mencacci, N. E., Topley, Lewis, Denny, P., Rizzu, P., Taba, P., Lovering, R., Ogalla, R. D., Foulger, R., Finkbeiner, S., Sveinbjornsdottir, S., Scholz, S., Koks, S., Foltynie, T., Price, T. R., Sheerin, U. -M., Williams, N., Reed, X., Wang, L., Brockmann, K., Oertel, W., Klein, C., Mohamed, F., Malard, L., Corti, O., Drouet, V., Goldwurm, S., Tesei, S., Canesi, M., Valente, E. M., Petrucci, S., Ginevrino, M., Toft, M., Aasly, J., Henriksen, S. P., Saetehaug, C., Orr-Urtreger, A., Giladi, N., Ferreira, J., Guedes, L. C., Bouca-Machado, R., Coelho, M., Rosa, M. M., Tolosa, E., Fernandez-Santiago, R., Ezquerra, M., Marti, M. J., Glaab, E., Balling, R., Chung, S. -J.

المصدر: Neurobiology of Aging
Neurobiology of aging 57, 247.e9-247.e13 (2017). doi:10.1016/j.neurobiolaging.2017.05.009

مصطلحات موضوعية: 0301 basic medicine, Aging, methods [Genome-Wide Association Study], 0302 clinical medicine, Corticobasal degeneration, neurodegenerative diseases, humans, risk, high-throughput screening assays, education.field_of_study, General Neuroscience, neurodegeneration, genetics [Genetic Variation], 3. Good health, Neurochip, alleles, methods [Genotyping Techniques], Frontotemporal dementia, Risk, Population, methods [High-Throughput Screening Assays], Computational biology, Genetic screening, genotyping, NeuroChip, NeuroX, apolipoproteins E, genetic variation, genome-wide association study, genotyping techniques, Article, Progressive supranuclear palsy, 03 medical and health sciences, Apolipoproteins E, medicine, Humans, Dementia, ddc:610, education, Genotyping, Alleles, business.industry, medicine.disease, 030104 developmental biology, genetics [Neurodegenerative Diseases], genetics [Apolipoproteins E], Neurology (clinical), Geriatrics and Gerontology, business, Neuroscience, 030217 neurology & neurosurgery, Imputation (genetics), Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c65471285ddf63c5acb2ebcd54d52517Test
https://doi.org/10.1016Test/j.neurobiolaging.2017.05.009

المؤلفون: Johansen, K., Jørgensen, J., Farrer, M., Aasly, J.

المصدر: Parkinsonism & Related Disorders ; volume 15, page S98-S99 ; ISSN 1353-8020

مصطلحات موضوعية: Neurology (clinical), Geriatrics and Gerontology, Neurology

الإتاحة: https://doi.org/10.1016/s1353-8020Test(09)70390-6
https://api.elsevier.com/content/article/PII:S1353802009703906?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S1353802009703906?httpAccept=text/plainTest

المؤلفون: Chartier-Harlin, M.-C., Dachsel, J., Hulihan, M., Kachergus, J., Lepretre, F., Le Rhun, E., Mutez, E., Lincoln, S., Ross, O., Vilariño-Güell, C., Yanagiya, A., Sonenberg, N., Lockhart, P., Wszolek, Z., Aasly, J., Frigerio, R., Maraganore, D., Lynch, T., Ferraris, A., Valente, E.-M., Destée, A., Farrer, M.

المصدر: Parkinsonism & Related Disorders ; volume 15, page S145-S146 ; ISSN 1353-8020

مصطلحات موضوعية: Neurology (clinical), Geriatrics and Gerontology, Neurology

الإتاحة: https://doi.org/10.1016/s1353-8020Test(09)70557-7
https://api.elsevier.com/content/article/PII:S1353802009705577?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S1353802009705577?httpAccept=text/plainTest

المؤلفون: Ross, O., Aasly, J., White, L., Gibson, J.M., Lynch, T., Uitti, R., Wszolek, Z., Lin, C.-H., Wu, R.-M., Farrer, M.

المصدر: Parkinsonism & Related Disorders ; volume 13, page S88 ; ISSN 1353-8020

مصطلحات موضوعية: Neurology (clinical), Geriatrics and Gerontology, Neurology

الإتاحة: https://doi.org/10.1016/s1353-8020Test(08)70579-0
https://api.elsevier.com/content/article/PII:S1353802008705790?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S1353802008705790?httpAccept=text/plainTest

المؤلفون: Heckman, Michael G, Elbaz, Alexis, Brighina, Laura, Pastor, Pao, Payami, Haydeh, Pchelina, Sofya N, Petersen, Maria Skaalum, Puschmann, Andrea, Ritz, Beate, Rogaeva, Ekaterina, Sazci, Ali, Slawek, Jaroslaw, Stefanis, Leonidas, Chartier-Harlin, Marie-Christine, Tan, Eng-King, Toda, Tatsushi, Toft, Mathias, Van Broeckhoven, Christine, Wirdefeldt, Karin, Woitalla, Dirk, Wszolek, Zbigniew K, Zimprich, Alexander, Dardiotis, Efthimios, Destée, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Fiske, Brian, Gispert, Suzana, Hadjigeorgiou, Georgios M, Hattori, Nobutaka, Soto-Ortolaza, Alexandra I, Ioannidis, John P A, Jasinska-Myga, Barbara, Jeon, Beom S, Kim, Yun Joong, Klein, Christine, Kruger, Rejko, Kyratzi, Elli, Lin, Chin-Hsien, Lohmann, Katja, Loriot, Marie-Anne, Serie, Daniel J, Lynch, Timothy, Mellick, George D, Mutez, Eugénie, Opala, Grzegorz, Park, Sung Sup, Petrucci, Simona, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A, Sohn, Young Ho, Aasly, Jan O, Tadic, Vera, Tomiyama, Hiroyuki, Uitti, Ryan J, Valente, Enza Maria, Vassilatis, Demetrios K, Vilariño-Güell, Carles, White, Linda R, Annesi, Grazia, Wu, Ruey-Meei, Xiromerisiou, Georgia, Maraganore, Demetrius M, Farrer, Matthew J, Ross, Owen A, Disease, Genetic Epidemiology Of Parkinson's, Auburger, Georg, Ioannidis, John P, Annesi, Grazie, Bentivoglio, Annarita, Bozi, Maria, Brice, Alexis, Carmine-Belin, Andrea, Carr, Jonathan, Bacon, Justin A, Carroll, Camille, Chase, Bruce, Checkoway, Harvey, Chen, Sheng-Di, Chung, Sun Ju, Cosentino, Carlos, Cresswell, Silke, Deutschlaender, Angela, Boczarska-Jedynak, Magdalena, Foroud, Tatiana, Garraux, Gaëtan, Goldwurm, Stefano, Hadjigeorgiou, George, Jeon, Beom Seok, Kawakami, Hideshi, Kishore, Asha, Krainc, Dimitri, Krygowska-Wajs, Anna, Lay-Son, Luis, Lin, Jeui-Jueng, Mellick, George, Morrison, Karen E, Munhoz, Renato P, Okubadejo, Njide U

المساهمون: Van Broeckhoven, Christine, Heckman, M, Elbaz, A, Soto Ortolaza, A, Serie, D, Aasly, J, Annesi, G, Auburger, G, Bacon, J, Boczarska Jedynak, M, Bozi, M, Brighina, L, Chartier Harlin, M, Dardiotis, E, Destée, A, Ferrarese, C, Ferraris, A, Fiske, B, Gispert, S, Hadjigeorgiou, G, Hattori, N, Ioannidis, J, Jasinska Myga, B, Jeon, B, Kim, Y, Klein, C, Kruger, R, Kyratzi, E, Lin, C, Lohmann, K, Loriot, M, Lynch, T, Mellick, G, Mutez, E, Opala, G, Park, S, Petrucci, S, Quattrone, A, Sharma, M, Silburn, P, Sohn, Y, Stefanis, L, Tadic, V, Tomiyama, H, Uitti, R, Valente, E, Vassilatis, D, Vilariño Güell, C, White, L, Wirdefeldt, K, Wszolek, Z, Wu, R, Xiromerisiou, G, Maraganore, D, Farrer, M, Ross, O

المصدر: Neurobiology of aging 35(1), 266.e5-266.e14 (2014). doi:10.1016/j.neurobiolaging.2013.07.013
Neurobiology of aging

مصطلحات موضوعية: Male, Aging, Parkinson's disease, european continental ancestry group, chemistry.chemical_compound, genetics [Parkinson Disease], Genotype, 80 and over, MAPT, genetics, genetics [Genetic Predisposition to Disease], Genetics, Aged, 80 and over, biology, General Neuroscience, LRRK2, Parkinson Disease, Middle Aged, Protein-Serine-Threonine Kinases, genetics [European Continental Ancestry Group], genetics [alpha-Synuclein], alpha-Synuclein, Medical genetics, Female, interaction, lrrk2, mapt, parkinson's disease, snca, adolescent, adult, aged, aged, 80 and over, asian continental ancestry group, female, genetic predisposition to disease, genotype, haplotypes, humans, leucine-rich repeat serine-threonine protein kinase-2, male, middle aged, parkinson disease, protein-serine-threonine kinases, risk, young adult, alpha-synuclein, tau proteins, genetic variation, Adult, Risk, medicine.medical_specialty, Interaction, Adolescent, Tau protein, MAPT protein, human, tau Proteins, Protein Serine-Threonine Kinases, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, genetics [Protein-Serine-Threonine Kinases], White People, Article, Young Adult, Genetic, Asian People, Genetic variation, genetics [Haplotypes], medicine, Humans, Genetic Predisposition to Disease, ddc:610, LRRK2 protein, human, SNCA protein, human, Biology, Aged, Alpha-synuclein, genetics [Asian Continental Ancestry Group], Haplotype, Genetic Variation, medicine.disease, nervous system diseases, genetics [tau Proteins], Haplotypes, chemistry, biology.protein, prevention & control [Parkinson Disease], SNCA, Neurology (clinical), Human medicine, Geriatrics and Gerontology, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a89d123fd093770f9b70adf4f21ecf7Test
https://pub.dzne.de/record/137120Test

المؤلفون: Ryan J. Uitti, Ekaterina Rogaeva, Anna Rita Bentivoglio, Hiroyuki Tomiyama, Ana Djarmati, Anthony E. Lang, Suzana Gispert, Owen A. Ross, Matthew J. Farrer, Marie-Christine Chartier-Harlin, Peter A. Silburn, Jan O. Aasly, Tatsushi Toda, J. Mark Gibson, Zbigniew K. Wszolek, Nadine Abahuni, Francesa de Nigris, George D. Mellick, Peter Lichtner, Manu Sharma, Carlo Ferrarese, Wataru Satake, Grzegorz Opala, Alain Destée, Aldo Quattrone, Demetrius M. Maraganore, Christine Van Broeckhoven, Suzanne Lesage, Chiara Riva, Jean-Charles Lambert, Olaf Riess, Karin Wirdefeldt, Nobutaka Hattori, Jessie Theuns, Timothy Lynch, John P. A. Ioannidis, Alexis Brice, Alexis Elbaz, Thomas Gasser, Rejko Krüger, Barbara Jasinska-Myga, Christine Klein, Grazia Annesi

المساهمون: Sharma, M, Maraganore, D, Ioannidis, J, Riess, O, Aasly, J, Annesi, G, Abahuni, N, Bentivoglio, A, Brice, A, Van Broeckhoven, C, Chartier Harlin, M, Destée, A, Djarmati, A, Elbaz, A, Farrer, M, Ferrarese, C, Gibson, J, Gispert, S, Hattori, N, Jasinska Myga, B, Klein, C, Lesage, S, Lynch, T, Lichtner, P, Lambert, J, Lang, A, Mellick, G, De Nigris, F, Opala, G, Quattrone, A, Riva, C, Rogaeva, E, Ross, O, Satake, W, Silburn, P, Theuns, J, Toda, T, Tomiyama, H, Uitti, R, Wirdefeldt, K, Wszolek, Z, Gasser, T, Krüger, R

المصدر: Neurobiology of aging
Neurobiology of aging 32(11), 2108.e1-2108.e5 (2011). doi:10.1016/j.neurobiolaging.2011.05.024

مصطلحات موضوعية: Aging, Candidate gene, Parkinson Disease/*genetics, genetics [Alcohol Oxidoreductases], Genotype, Genetic Loci/*genetics, Population, education, sepiapterin reductase, SPR, Single-nucleotide polymorphism, Locus (genetics), Genetic Association Studie, genetics [Genetic Loci], Biology, Polymorphism, Single Nucleotide, Alcohol Oxidoreductase, PD genetic studies, genetics [Parkinson Disease], PARK3, Humans, Genetic Predisposition to Disease, ddc:610, Sepiapterin reductase, Promoter Regions, Genetic, Gene, Alcohol Oxidoreductases/*genetics, Genetic Association Studies, Genetics, education.field_of_study, General Neuroscience, Odds ratio, Parkinson disease, Alcohol Oxidoreductases, Settore MED/26 - NEUROLOGIA, Genetic epidemiology, Genetic Loci, Neurology (clinical), Human medicine, Geriatrics and Gerontology, Human, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39c2e3ba82867adf2da33c5438d6ddacTest
http://olympias.lib.uoi.gr/jspui/handle/123456789/18509Test

المؤلفون: Demetrius M. Maraganore, Suzanne Lesage, Christine Klein, Ana Djarmati, Alessandro Prigione, Georgia Xiromerisiou, Aldo Quattrone, Christine Van Broeckhoven, Thomas Gasser, Nobutaka Hattori, Jan O. Aasly, Eng-King Tan, Anna Rita Bentivoglio, Alexis Brice, Zbigniew K. Wszolek, Carlo Ferrarese, Grazia Annesi, Grzegorz Opala, Hiroyuki Tomiyama, Wataru Satake, Owen A. Ross, J. Mark Gibson, Peter A. Silburn, Georgios M. Hadjigeorgiou, Matthew J. Farrer, Alexis Elbaz, Jean-Charles Lambert, Olaf Riess, Karin Wirdefeldt, George D. Mellick, Barbara Jasinska-Myga, Juei-Jueng Lin, Timothy Lynch, Jessie Theuns, Rejko Krüger, Manu Sharma, Francesa de Nigris, John P. A. Ioannidis, Tatsushi Toda

المساهمون: Krüger, R, Sharma, M, Riess, O, Gasser, T, Van Broeckhoven, C, Theuns, J, Aasly, J, Annesi, G, Bentivoglio, A, Brice, A, Djarmati, A, Elbaz, A, Farrer, M, Ferrarese, C, Gibson, J, Hadjigeorgiou, G, Hattori, N, Ioannidis, J, Jasinska Myga, B, Klein, C, Lambert, J, Lesage, S, Lin, J, Lynch, T, Mellick, G, de Nigris, F, Opala, G, Prigione, A, Quattrone, A, Ross, O, Satake, W, Silburn, P, Tan, E, Toda, T, Tomiyama, H, Wirdefeldt, K, Wszolek, Z, Xiromerisiou, G, Maraganore, D, for the Genetic Epidemiology of Parkinson's disease, C, Pathologic Biochemistry and Physiology, Pollak, Pierre

المصدر: Neurobiology of aging (2011).
info:cnr-pdr/source/autori:Krüger R, Sharma M, Riess O, Gasser T, Van Broeckhoven C, Theuns J, Aasly J, Annesi G, Bentivoglio AR, Brice A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Jasinska-Myga B, Klein C, Lambert JC, Lesage/titolo:A large-scale genetic association study to evaluate the contribution of Omi%2FHtrA2 (PARK13) to Parkinson's disease/doi:/rivista:Neurobiology of aging/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volume
Neurobiology of aging 32 (2010): 548e9–548e18. doi:10.1016/j.neurobiolaging.2009.11.021
info:cnr-pdr/source/autori:Krüger R, Sharma M, Riess O, Gasser T, Van Broeckhoven C, Theuns J, Aasly J, Annesi G, Bentivoglio AR, Brice A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Jasinska-Myga B, Klein C, Lambert JC, Lesage/titolo:A large-scale genetic association study to evaluate the contribution of Omi%2FHtrA2 (PARK13) to Parkinson's disease./doi:10.1016%2Fj.neurobiolaging.2009.11.021/rivista:Neurobiology of aging/anno:2010/pagina_da:548e9/pagina_a:548e18/intervallo_pagine:548e9–548e18/volume:32
Neurobiology of aging
Neurobiology of Aging, Vol. 32, No 3 (2011) pp. 548.e9-18

مصطلحات موضوعية: Male, Aging, Parkinson Disease/epidemiology/*ethnology/*genetics, Polymorphism, Single Nucleotide/*genetics, International Cooperation, Serine Endopeptidases/*genetics, Genome-wide association study, Bioinformatics, Cohort Studies, Gene Frequency, Neuropathology, Medicine(all), General Neuroscience, Parkinson Disease/epidemiology/ethnology/genetics, Serine Endopeptidases, Mitochondrial Proteins/*genetics, Parkinson Disease, High-Temperature Requirement A Serine Peptidase 2, Middle Aged, Random effects model, Polymorphism, Single Nucleotide/genetics, Mitochondrial Proteins/genetics, Female, European Continental Ancestry Group/ethnology, Genotype, Single-nucleotide polymorphism, Serine Endopeptidases/genetics, Biology, Polymorphism, Single Nucleotide, Parkinson Disease/epidemiology, White People, Article, Mitochondrial Proteins, Meta-Analysis as Topic, Humans, Genetic Predisposition to Disease, Allele frequency, Genetic association, Aged, MED/26 - NEUROLOGIA, Chi-Square Distribution, Odds ratio, ddc:616.8, Malattia di Parkinson, PARK13, genetica, Genetic epidemiology, Multiple comparisons problem, Neurology (clinical), Human medicine, Geriatrics and Gerontology, Developmental Biology, Demography, Genome-Wide Association Study

وصف الملف: application/msword; pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4520065a94a4f8f11b9c06471281f32dTest
http://hdl.handle.net/10281/8560Test